Canonical Allele Identifier: PA2825224712
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Arg125Cys
CA004443
NM_001001432.3:c.373C>T